Fighting for Access and Awareness With Dreamsickle Kids

from Wait, How Do You Spell That? A Rare Disease Podcast · host waithowdoyouspellthatraredisease

Colby speaks with Gina Glass, the founder of the Dreamsickle Kids Foundation in Nevada. Her sickle cell disease organization has helped to raise awareness and form legislation centered around access in that state. Gina speaks about her ongoing efforts, how to support family members with sickle cell, and what's on the horizon. Find out more at www.dreamsicklekids.org.

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This episode was published on February 5, 2021.

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